Related Conditions
Trisomy 21- meiotic nondisjunction(child)
Trisomy 21- mitotic nondisjunction mosaicism(child)
Myeloid leukemia co-occurrent with Down syndrome(child)
Transient abnormal myelopoiesis co-occurrent with Down syndrome(child)
Dementia with Down syndrome(child)
Down syndrome co-occurrent with leukemoid reaction associated transient neonatal pustulosis(child)
Translocation Down syndrome(child)
Trisomy and partial trisomy of autosome(parent)
Anomaly of chromosome pair 21(parent)
Congenital malformation(parent)
Quick Facts
- SNOMED CT
- 41040004
- UMLS CUI
- C4521042
- Fully Specified Name
- Complete trisomy 21 syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.